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一个丝氨酸激酶转化基因的表达性cDNA克隆

Expression cDNA cloning of a serine kinase transforming gene.

作者信息

Chan A M, Chedid M, McGovern E S, Popescu N C, Miki T, Aaronson S A

机构信息

Laboratory of Cellular and Molecular Biology, National Cancer Institute, Bethesda, Maryland 20892.

出版信息

Oncogene. 1993 May;8(5):1329-33.

PMID:8479752
Abstract

By ectopic expression of cDNAs derived from a Ewing sarcoma cell line in NIH3T3 cells, we isolated a transforming gene (est). Sequence analysis revealed homology to the cot oncogene, which encodes a novel serine kinase. Whereas the cot product was truncated at its carboxy-terminal end as a result of gene rearrangement during transfection, est encodes the normal cot product. Thus, this gene can be activated as an oncogene by overexpression as well as by gene rearrangement. NIH3T3 cells transfected with est formed progressively growing colonies in soft agar and were tumorigenic in nude mice. The 3.2-kb est transcript was expressed at low level in both human fibroblasts and epithelial cells. Addition of the tumor promoter, okadaic acid (OA), or cytokine, interleukin 1 (IL-1), but not serum or platelet-derived growth factor (PDGF), induced increased expression of the est transcript. Using fluorescence in situ hybridization, we localized the est gene to the short arm of human chromosome 10 at band p11.2.

摘要

通过在NIH3T3细胞中异位表达源自尤因肉瘤细胞系的cDNA,我们分离出了一个转化基因(est)。序列分析显示其与cot癌基因具有同源性,cot癌基因编码一种新型丝氨酸激酶。虽然由于转染过程中的基因重排,cot产物在其羧基末端被截短,但est编码正常的cot产物。因此,该基因可通过过表达以及基因重排被激活成为癌基因。用est转染的NIH3T3细胞在软琼脂中形成逐渐生长的集落,并且在裸鼠中具有致瘤性。3.2kb的est转录本在人成纤维细胞和上皮细胞中均低水平表达。添加肿瘤启动子冈田酸(OA)或细胞因子白细胞介素1(IL-1),而非血清或血小板衍生生长因子(PDGF),可诱导est转录本表达增加。利用荧光原位杂交技术,我们将est基因定位到人类染色体10短臂的p11.2带。

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